Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g60640 | A03 | 30492127 | C | T | upstream_gene_variant | MODIFIER | c.-4353C>T| |
S292 |
2 | BAA03g60640 | A03 | 30493286 | G | A | upstream_gene_variant | MODIFIER | c.-3194G>A| |
S269 |
3 | BAA03g60640 | A03 | 30494536 | C | T | upstream_gene_variant | MODIFIER | c.-1944C>T| |
S30 S31 |
4 | BAA03g60640 | A03 | 30494605 | C | T | upstream_gene_variant | MODIFIER | c.-1875C>T| |
S20 |
5 | BAA03g60640 | A03 | 30494699 | C | T | upstream_gene_variant | MODIFIER | c.-1781C>T| |
S234 |
6 | BAA03g60640 | A03 | 30495026 | C | T | upstream_gene_variant | MODIFIER | c.-1454C>T| |
S225 S73 |
7 | BAA03g60640 | A03 | 30495309 | G | T | upstream_gene_variant | MODIFIER | c.-1171G>T| |
S284 |
8 | BAA03g60640 | A03 | 30496033 | C | T | upstream_gene_variant | MODIFIER | c.-447C>T| |
S174 |
9 | BAA03g60640 | A03 | 30496965 | C | T | missense_variant | MODERATE | c.376C>T|p.Pro126Ser |
S207 |
10 | BAA03g60640 | A03 | 30497609 | C | T | synonymous_variant | LOW | c.762C>T|p.Ile254Ile |
S280 |
11 | BAA03g60640 | A03 | 30498059 | C | T | downstream_gene_variant | MODIFIER | c.*399C>T| |
S232 |